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Quoted phrase not found in phrase index: "Spermatogenic failure 14"
Page 1
Genetic causes of spermatogenic failure.
Massart A, Lissens W, Tournaye H, Stouffs K. Massart A, et al. Asian J Androl. 2012 Jan;14(1):40-8. doi: 10.1038/aja.2011.67. Epub 2011 Dec 5. Asian J Androl. 2012. PMID: 22138898 Free PMC article. Review.
Large-scale analyses of the X chromosome in 2,354 infertile men discover recurrently affected genes associated with spermatogenic failure.
Riera-Escamilla A, Vockel M, Nagirnaja L, Xavier MJ, Carbonell A, Moreno-Mendoza D, Pybus M, Farnetani G, Rosta V, Cioppi F, Friedrich C, Oud MS, van der Heijden GW, Soave A, Diemer T, Ars E, Sánchez-Curbelo J, Kliesch S, O'Bryan MK, Ruiz-Castañe E; GEMINI Consortium; Azorín F, Veltman JA, Aston KI, Conrad DF, Tüttelmann F, Krausz C. Riera-Escamilla A, et al. Am J Hum Genet. 2022 Aug 4;109(8):1458-1471. doi: 10.1016/j.ajhg.2022.06.007. Epub 2022 Jul 8. Am J Hum Genet. 2022. PMID: 35809576 Free PMC article.
Collectively, our study represents a significant step towards the definition of the missing genetic etiology in idiopathic severe spermatogenic failure and significantly reduces the knowledge gap of X-linked genetic causes of azoospermia/cryptozoospermia contributin …
Collectively, our study represents a significant step towards the definition of the missing genetic etiology in idiopathic severe spermat
Systematic molecular analyses for 115 karyotypically normal men with isolated non-obstructive azoospermia.
Muranishi Y, Kobori Y, Katoh-Fukui Y, Tamaoka S, Hattori A, Osaka A, Okada H, Nakabayashi K, Hata K, Kawai T, Ogata-Kawata H, Iwahata T, Saito K, Kon M, Shinohara N, Fukami M. Muranishi Y, et al. Hum Reprod. 2024 May 2;39(5):1131-1140. doi: 10.1093/humrep/deae057. Hum Reprod. 2024. PMID: 38511217
This frequency is higher than that of the reference data in Japan and China (11.1% and 14.7%, respectively). Known NOA-causative AZF-linked CNVs were found in nine (7.8%) cases. ...These results broadened the structural variations of AZF-linked CNVs, which should be consid …
This frequency is higher than that of the reference data in Japan and China (11.1% and 14.7%, respectively). Known NOA-causative AZF- …
Copy number variations in spermatogenic failure patients with chromosomal abnormalities and unexplained azoospermia.
Dong Y, Pan Y, Wang R, Zhang Z, Xi Q, Liu RZ. Dong Y, et al. Genet Mol Res. 2015 Dec 7;14(4):16041-9. doi: 10.4238/2015.December.7.17. Genet Mol Res. 2015. PMID: 26662397 Free article.
Spermatogenic failure patients consisting of 13 males with chromosomal abnormalities and 20 with unexplained azoospermia were enrolled. ...By applying high throughput genome-wide sequencing to determine CNVs, we provide a number of candidate genes possibly contribut
Spermatogenic failure patients consisting of 13 males with chromosomal abnormalities and 20 with unexplained azoospermia were
Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes.
Chen S, Wang G, Zheng X, Ge S, Dai Y, Ping P, Chen X, Liu G, Zhang J, Yang Y, Zhang X, Zhong A, Zhu Y, Chu Q, Huang Y, Zhang Y, Shen C, Yuan Y, Yuan Q, Pei X, Cheng CY, Sun F. Chen S, et al. Hum Mol Genet. 2020 Aug 11;29(14):2451-2459. doi: 10.1093/hmg/ddaa101. Hum Mol Genet. 2020. PMID: 32469048
Rare coding variants have been proven to be one of the significant factors contributing to spermatogenic failure in patients with non-obstructive azoospermia (NOA) and severe oligospermia (SO). ...
Rare coding variants have been proven to be one of the significant factors contributing to spermatogenic failure in patients w …
Testicular Growth and Pubertal Onset in GH-Deficient Children Treated With Growth Hormone: A Retrospective Study.
Cannarella R, Caruso M, Crafa A, Timpanaro TA, Lo Bianco M, Presti S, Condorelli RA, La Vignera S, Calogero AE. Cannarella R, et al. Front Endocrinol (Lausanne). 2021 Apr 2;12:619895. doi: 10.3389/fendo.2021.619895. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 33868165 Free PMC article.
An Italian survey has reported bilateral testicular hypotrophy in 14% of final-year high school students. The search for determinants of testicular growth in childhood is important for the primary prevention of spermatogenic failure. ...
An Italian survey has reported bilateral testicular hypotrophy in 14% of final-year high school students. The search for determinants …
Exosomal microRNAs in seminal plasma are markers of the origin of azoospermia and can predict the presence of sperm in testicular tissue.
Barceló M, Mata A, Bassas L, Larriba S. Barceló M, et al. Hum Reprod. 2018 Jun 1;33(6):1087-1098. doi: 10.1093/humrep/dey072. Hum Reprod. 2018. PMID: 29635626 Free PMC article.
This study compares the miRNA content of exosomes in semen samples obtained from nine normozoospermic fertile individuals (control group), 14 infertile men diagnosed with azoospermia due to spermatogenic failure, and 13 individuals with obstructive azoospermi …
This study compares the miRNA content of exosomes in semen samples obtained from nine normozoospermic fertile individuals (control group), …
Chromosomal abnormality and Y chromosome microdeletion in Chinese patients with azoospermia or severe oligozoospermia.
Zhou-Cun A, Yang Y, Zhang SZ, Zhang W, Lin L. Zhou-Cun A, et al. Yi Chuan Xue Bao. 2006 Feb;33(2):111-6. doi: 10.1016/s0379-4172(06)60029-2. Yi Chuan Xue Bao. 2006. PMID: 16529294
Chromosomal abnormality and Y chromosome microdeletion are regarded as two frequent genetic causes associated with spermatogenic failure in Caucasian population. To investigate the distribution of the two genetic defects in Chinese patients with azoospermia or sever …
Chromosomal abnormality and Y chromosome microdeletion are regarded as two frequent genetic causes associated with spermatogenic f
Edward Martin (1859-1938). The founding father of modern clinical andrology.
Jequier AM. Jequier AM. Int J Androl. 1991 Feb;14(1):1-10. doi: 10.1111/j.1365-2605.1991.tb01057.x. Int J Androl. 1991. PMID: 2007522
He pointed out the need for semen analysis in diagnosis and also demonstrated that azoospermia could have two causes, namely spermatogenic failure and ductal obstruction. He also made some important observations on sperm movement. ...
He pointed out the need for semen analysis in diagnosis and also demonstrated that azoospermia could have two causes, namely spermatogeni